Canonical Allele Identifier: CA2117826564
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1880493403
gnomAD v4: 13-108267187-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267187C>A , CM000675.2:g.108267187C>A GRCh38
NC_000013.10:g.108919535C>A , CM000675.1:g.108919535C>A GRCh37
NC_000013.9:g.107717536C>A NCBI36
NG_029524.1:g.2559C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000486502.1:n.78-2913C>A
XR_931715.1:n.1822C>A
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